A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702277



Internal ID15438929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90090173..90094483hg38UCSC Ensembl
Innerchr7:89719487..89723797hg19UCSC Ensembl
Innerchr7:89557423..89561733hg18UCSC Ensembl
Innerchr7:89364138..89368448hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg384311
hg194311
hg184311
hg174311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702277
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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